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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
congenital dyserythropoietic anemia +   
A congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood. (DO)
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital nonspherocytic hemolytic anemia +   
dehydrated hereditary stomatocytosis +   
glucosephosphate dehydrogenase deficiency +   
hemoglobinopathy +   
hereditary elliptocytosis +   
hereditary spherocytosis +   
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
overhydrated hereditary stomatocytosis  
Red Cell Phospholipid Defect with Hemolysis 
Rh-Null Disease, Amorph Type  
sickle cell anemia +   
Stomatocytosis II  
Transient Erythroblastopenia of Childhood 
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  
X-linked congenital hemolytic anemia  

Synonyms
Exact Synonyms: Congenital Dyserythropoietic Anemias ;   congenital dyshaematopoietic anaemia
Broad Synonyms: syndromic congenital hemolytic and dyserythropoietic anemia
Primary IDs: MESH:D000742
Xrefs: GARD:1999 ;   ICD10CM:D64.4 ;   NCI:C84646 ;   OMIM:PS224120 ;   ORDO:85
Definition Sources: http://en.wikipedia.org/wiki/Congenital_dyserythropoietic_anemia "DO" "DO", http://www.ncbi.nlm.nih.gov/books/NBK5313/ "DO" "DO"

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